Evidence map›Paper›PMID 21793850›Full record

ReviewAnnals of the New York Academy of Sciences2011

Assessing estrogen signaling aberrations in breast cancer risk using genetically engineered mouse models.

Priscilla A Furth, M Carla Cabrera, Edgar S Díaz-Cruz, Sarah Millman, Rebecca E Nakles

Open access · bronzeAbstract readReview
In one paragraph

Review in Annals of the New York Academy of Sciences, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 29% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Tamoxifen Resistance: Emerging Molecular Targets.International journal of molecular sciences · 2016
    Review
  8. Review
  9. Article
  10. Article
  11. Microbiome as a Target for Cancer Therapy.Integrative cancer therapies
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Priscilla A FurthDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA. paf3@georgetown.edu
M Carla Cabrera
Edgar S Díaz-Cruz
Sarah Millman
Rebecca E Nakles
Georgetown University Medical Center · USGeorgetown University · US

Funding

TRAINING GRANT IN TUMOR BIOLOGYT32CA009686 · NCI · GEORGETOWN UNIVERSITY · PI ANNA Tate RIEGEL, DAVID J ROBBINS · 1996 to 2026
$10.8M
Mechanisms of RET/PTC rearrangements in thyroid cancerR01CA088041 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI NIKIFOROV, YURI E · 2001 to 2017
$3.8M
Progression and regression of mammary preneoplasiaR01CA112176 · NCI · GEORGETOWN UNIVERSITY · PI FURTH, PRISCILLA A. · 2005 to 2018
$3.1M
MECHANISMS REGULATING REVERSAL OF PREMALIGNANCYR01CA089041 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI FURTH, PRISCILLA A. · 2001 to 2009
$2.0M
NCI NIH HHS 2R01 CA88041NCI NIH HHS 2R01CA88041-1OS1NCI NIH HHS R01 CA088041NCI NIH HHS R01 CA089041NCI NIH HHS R01 CA112176NCI NIH HHS T32 CA009686
6 · The paper itself

Abstract

Aberrations in estrogen signaling increase breast cancer risk. Molecular mechanisms that impact breast cancer initiation, promotion, and progression can be investigated using genetically engineered mouse models. Increasing estrogen receptor alpha (ERα) expression levels twofold is sufficient to initiate and promote breast cancer progression. Initiation and promotion can be increased by p53 haploinsufficiency and by coexpressing the nuclear coactivators amplified in breast cancer 1 (AIB1) or the splice variant AIB1Δ3. Progression to invasive cancer is found with coexpression of these nuclear coactivators as well as following a single dose of 7,12-dimethylbenz(a)anthracene. Loss of signal transducer and activator of transcription 5a reduces the prevalence of initiation and promotion but does not protect from invasive cancer development. Cyclin D1 loss completely interrupts mammary epithelial proliferation and survival when ERα is overexpressed. Loss of breast cancer gene 1 increases estrogen signaling and cooperates with ERα overexpression in initiation, promotion, and progression of mammary cancer.

Indexed as

Signal TransductionAnimalsBreast NeoplasmsEstrogen Receptor alphaEstrogensFemaleGenetic EngineeringMiceRisk FactorsEstrogen Receptor alphaEstrogens

Identifiers

PMID21793850
PMCPMC3154027
OpenAlexW1540182210

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.